Delavaux Camille S, Bever James D, Karppinen Erin M, Bainard Luke D
Department of Ecology and Evolutionary Biology The University of Kansas Lawrence KS USA.
Kansas Biological Survey The University of Kansas Lawrence KS USA.
Ecol Evol. 2020 Mar 31;10(11):4652-4664. doi: 10.1002/ece3.6219. eCollection 2020 Jun.
With the advances of sequencing tools, the fields of environmental microbiology and soil ecology have been transformed. Today, the unculturable majority of soil microbes can be sequenced. Although these tools give us tremendous power and open many doors to answer important questions, we must understand how sample processing may impact our results and interpretations. Here, we test the impacts of four soil storage methods on downstream amplicon metabarcoding and qPCR analyses for fungi and bacteria. We further investigate the impact of thaw time on extracted DNA to determine a safe length of time during which this can occur with minimal impact on study results. Overall, we find that storage using standard cold packs with subsequent storage at -20°C is little different than immediate storage in liquid nitrogen, suggesting that the historical and current method is adequate. We further find evidence that storage at room temperature or with aid of RNAlater can lead to changes in community composition and in the case of RNAlater, lower gene copies. We therefore advise against these storage methods for metabarcoding analyses. Finally, we show that over 1 month, DNA extract thaw time does not impact diversity or qPCR metrics. We hope that this work will help researchers working with soil bacteria and fungi make informed decisions about soil storage and transport to ensure repeatability and accuracy of results and interpretations.
随着测序技术的进步,环境微生物学和土壤生态学领域发生了变革。如今,大多数无法培养的土壤微生物都可以进行测序。尽管这些技术赋予我们巨大的能力,为解答重要问题打开了许多大门,但我们必须了解样本处理可能如何影响我们的结果和解释。在此,我们测试了四种土壤储存方法对下游真菌和细菌扩增子元条形码分析及定量聚合酶链反应(qPCR)分析的影响。我们进一步研究了解冻时间对提取的DNA的影响,以确定在此期间能够发生且对研究结果影响最小的安全时长。总体而言,我们发现使用标准冷敷袋储存随后在-20°C下储存与立即储存在液氮中几乎没有差异,这表明历史上和当前的方法是足够的。我们还进一步发现证据表明,在室温下储存或借助RNA Later储存会导致群落组成发生变化,而就RNA Later而言,基因拷贝数会降低。因此,我们建议不要将这些储存方法用于元条形码分析。最后,我们表明在超过1个月的时间里,DNA提取物的解冻时间不会影响多样性或qPCR指标。我们希望这项工作将帮助研究土壤细菌和真菌的研究人员在土壤储存和运输方面做出明智的决策,以确保结果和解释的可重复性和准确性。